Effect of prior oxidation on the creep behavior of NiAl-hardened austenitic steel

The effect of prior oxidation at 1473 K on the creep behavior of an Fe-Ni-Cr-Al alloy, hardened by ordered NiAl precipitates, has been investigated at 873 K over a stress range of 275 to 450 MPa. The alloy in the as-electroslag remelted (ESR) as well as the ESR-plus-hot-worked conditions was considered. Prior oxidation causes creep strengthening in the Fe-Ni-Cr-Al alloy, resulting in a decrease in minimum creep rate and increase in time to rupture, in contrast to the observations reported on nickel-based superalloys. Creep strengthening is, however, accompanied by a significant reduction in creep ductility. Oxidation-induced creep strengthening in the current alloy can be attributed to the improved adherence of surface oxide caused by the presence of yttrium. An effective stress that incorporates the contributions of load transfer as well as substructural strengthening is used to account for the observed oxidation-induced creep strengthening. While creep strengthening is more pronounced in the ESR cast alloy, the loss in creep ductility is more intense in the ESR wrought alloy. Increasing the oxidation time beyond 1 hour has a minimal effect on creep strengthening of both the alloys, though it lowers significantly the creep ductility of the wrought alloy. The observed differences in creep behavior of the alloy in the two different conditions could be attributed to the differences in grain size as well as morphology and related oxidation-induced damage.     

Nuclear-chemical synthesis of tritium-labeled phenyl-substituted picoline derivatives

Ion-molecule reactions of free phenyl cations with six-membered nitrogen-containing heterocyclic compounds: α-, β-, and γ-picolines, were studied. Phenyl cations were generated by tritium β-decay in double-labeled benzene. The mechanism of competing reactions of electrophilic addition to the nitrogen heteroatom in the ring and electrophilic substitution of the C-H bond in the pyridine ring was examined. The effect of methyl substituent in the pyridine molecule on the reaction pathway was evaluated. A one-step procedure for nuclear-chemical synthesis of tritium-labeled N-phenylpicolinium salts and phenyl-substituted picolines was developed.     

高频微型脉冲管制冷机的实用化研究

脉冲管制冷机经过多年的发展，性能不断改善，目前已开始进入实用化阶段。高频微型脉冲管制冷机结构紧凑，应用方便，并且主要工作在需求量较大的液氮温区，因此将首先得到一定规模的应用。介绍了作者针对脉冲管制冷机在红外和超导方面的应用所作的实用化工作，讨论了尚待解决的问题。     

Mutual recognition of the results of measurements and tests and formation of a world-wide metrology system

The main prerequisites are considered in a historical aspect and steps ate taken in creating a world-wide metrology system with the aim of providing conditions for the mutual recognition of measurement results. __________ Translated from Izmeritel’naya Tekhnika, No. 11. pp. 59–62, November, 2007.     

Radiation-induced hydrogen yield from silicon bombarded with 710-MeV bismuth ions

The behavior of hydrogen in solids under the action of intense ionizing radiation is of importance in solving numerous problems of materials science for the nuclear and thermonuclear power industry, spacecraft engineering, hydrogen energetics, and microelectronics. Experimental results are presented that provide evidence of the radiation-induced yield of hydrogen from single crystal silicon bombarded with 710-MeV bismuth ions.     

Synthesis and Properties of Photoisomerizable Derivatives of Isosorbide and Their Use in Cholesteric Filters

This paper describes the synthesis of photoisomerizable derivatives of isosorbide. These derivatives contain a stilbene or cinnamate moiety and can therefore be used as photoisomerizable chiral compounds in cholesteric liquid‐crystalline mixtures. The reflection wavelength of cholesteric layers made from these mixtures is increased by UV irradiation due to the fact that the Z‐isomers of these derivatives exhibit a lower helical twisting power than the corresponding E‐isomers. The cinnamate derivatives are very suitable for use in cholesteric color filters that find application in liquid‐crystal displays.     

Effects of reducing and oxidizing atmospheres on the PTCR characteristics of porous n-BaTiO3 ceramics by adding polyethylene glycol

Donor doped BaTiO₃ (n-BaTiO₃) ceramics were fabricated by adding polyethylene glycol (PEG) at 20 wt %. The effects of reducing and oxidizing atmospheres on the PTCR characteristics of the porous n-BaTiO₃ ceramics were investigated. The PTCR characteristics of the porous n-BaTiO₃ ceramics is strongly affected by chemisorbed oxygen at the grain boundaries and are recovered as the atmosphere is changed from the reducing gas to oxidizing gas. The low room-temperature resistivity of the porous n-BaTiO₃ ceramics in reducing atmospheres may be caused by the decrease in potential barrier height, which originates from an increase in the number of electrons owing to the desorption of chemisorbed oxygen atoms at the grain boundaries. In addition, the high room-temperature resistivity of the porous n-BaTiO₃ ceramics in oxidizing atmospheres may be caused by the increase in potential barrier height, which results from the adsorption of chemisorbed oxygen atoms at the grain boundaries.     

GaAs pHEMT-based technology for microwave applications in a volume MMIC production environment on 150-mm wafers

The establishment of a 150-mm (6-in) gallium arsenide (GaAs) facility is described together with the development of very high yielding and cost-effective semiconductor device technologies and a manufacturing capacity of over 40000 wafers/annum. The background to the demand for very high volumes of RF products for this market is discussed, together with the prospects for future growth. The paper describes recent process development by the utilization of a data-driven yield management system to support the delivery of high-quality RF products to customers. Finally, "end of line" DC and RF testing of finished 150-mm GaAs pHEMT foundry wafers is described, enabling scalar measurements of power, noise, and intermodulation products as well as vector measurements of S-parameters and noise parameters at frequencies of up to 40 GHz.     

Time stepping schemes for coupled displacement and pore pressurē analysis

 The paper investigates the performance of various time stepping schemes for coupled displacement and pore pressure analysis. A number of alternative forms of the automatic time stepping method proposed by Sloan and Abbo (1999a) are also presented. These alternative schemes use different updates for the displacements and pore pressures and also adopt different starting conditions for the iterations. The automatic schemes are compared with an implicit θ-method, as well as an explicit method, through analysis of a variety of problems involving undrained loading, drained loading, and consolidation for Mohr-Coulomb and critical state models. As expected, the numerical results confirm that the explicit scheme is neither accurate nor robust. Although the implicit θ-method is accurate and fast, it fails to give a solution in a number of cases where the time step is large. The automatic schemes are shown to be accurate, fast and generally robust. Two of the automatic schemes proposed never fail to furnish a solution for the cases considered. In addition, all the automatic schemes are able to constrain the time-stepping (temporal integration) error in the displacements and pore pressures to lie near a prescribed tolerance, provided the iteration error tolerance is properly chosen. For complex soil models, it is important that the latter is set sufficiently small in order for the schemes to be able to constrain the time-stepping error to lie within a prescribed tolerance. Dedicated to the memory of Prof. Mike Crisfield, for his cheerfulness and cooperation as a colleague and friend over many years.     

Changes in polymer foils used in food packaging tested by using differential scanning calorimetry

This work is an experimental study of the differential scanning calorimetry characterisation of polymer materials used in food packaging materials, such as polypropylene (0.03 mm), polyethylene (0.1 and 0.03 mm), poly(D-(-)-Β-hydroxybutyrate) (powder), two-layered polypropylene (0.064 mm), and two-layered polypropylene with poly-vinylidene-chloride (0.012/0.021). The polymer stability was checked by simulation of conditions during food preparation in microwave ovens, sterilisation or rapid freezing. The materials were tested in the temperature range from 40 to 200‡C at different scan rates from 2 to 30°C min⁻¹ during heating or cooling. The enthalpies show a high correlation coefficient (0.964) with scan rate. All samples undergo phase change in the temperature range from 107 to 173°C during heating and enthalpies are in the range from 31.8 to 71.1Jg⁻¹. Upon subsequent cooling from 200°C, the temperature range of phase changes is shifted to lower temperatures from 86 to 102°C with enthalpies ranging from 30.4 to 57.8 J g⁻¹. Experiments with exposure of polymers to microwave radiation and freezing prove that the phase change considering the temperature range is very similar in all experiments.